Mesenchymal Stem Cells: a Promising Therapeutic Tool for Acute Kidney Injury

被引:22
|
作者
Selim, Rehab E. [1 ,2 ]
Ahmed, Hanaa H. [1 ,2 ]
Abd-Allah, Somia H. [3 ]
Sabry, Gilane M. [4 ]
Hassan, Rasha E. [4 ]
Khalil, Wagdy K. B. [5 ]
Abouhashem, Nehal S. [6 ]
机构
[1] Natl Res Ctr, Hormones Dept, Giza, Egypt
[2] Natl Res Ctr, Ctr Excellence Adv Sci, Stem Cell Lab, Giza, Egypt
[3] Zagazig Univ, Fac Med, Med Biochem & Mol Biol Dept, Zagazig, Egypt
[4] Ain Shams Univ, Biochem Dept, Fac Sci, Cairo, Egypt
[5] Natl Res Ctr, Cell Biol Dept, Giza, Egypt
[6] Zagazig Univ, Fac Med, Pathol Dept, Zagazig, Egypt
关键词
Acute kidney injury; Cisplatin; Mesenchymal stem cells; Oxidative stress; Apoptosis; Angiogenesis; ENDOTHELIAL GROWTH-FACTOR; CISPLATIN-INDUCED NEPHROTOXICITY; CONVERTING ENZYME-INHIBITOR; BONE-MARROW; SIGNALING PATHWAY; CYSTATIN-C; CARDIOMYOCYTE APOPTOSIS; RECEPTOR BLOCKER; ADIPOSE-TISSUE; PROTEIN-KINASE;
D O I
10.1007/s12010-019-02995-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acute kidney injury (AKI) is a rapid loss of renal function. It has high mortality rates. Still, renal replacement therapy is considered the best solution for recovering AKI. This opens a line of thought to develop an alternative therapy for it without complications. Mesenchymal stem cells are considered a new therapy for treating kidney diseases. The aim of this work was to address the anti-apoptotic, antioxidative, and pro-angiogenic effects of adipose tissue-derived MSCs (AD-MSCs) and bone marrow-MSCs (BM-MSCs) for treating AKI. Adult male Wistar rats were assigned into nine groups (n = 10): (1) the control group; (2) the AKI group, receiving cisplatin; (3) the AKI group treated with AD-MSCs (1 x 10(6)); (4) the AKI group treated with AD-MSCs (2 x 10(6)); (5) the AKI group treated with AD-MSCs (4 x 10(6)); (6) the AKI group treated with losartan; (7) the AKI group treated with BM-MSCs (1 x 10(6)); (8) the AKI group treated with BM-MSCs (2 x 10(6)); and (9) the AKI group treated with BM-MSCs (4 x 10(6)). The results showed a significant rise in creatinine, urea, and cystatin C (cys C) levels and upregulation of p38 mRNA, whereas a significant decline in NAD(P)H quinone oxidoreductase 1 (NQO-1) protein and downregulation of B-cell lymphoma-2 (Bcl-2) mRNA and vascular endothelial growth factor (VEGF) mRNA were recorded in AKI. MSCs could improve renal functions manifested by decreased urea, creatinine, and cys C levels; downregulation of p38; and upregulation of Bcl-2 and VEGF. Moreover, MSC therapy could induce NQO-1 in the treated rats relative to the untreated rats. So, cell-based therapy can reduce AKI through the antioxidative, anti-apoptotic, and pro-angiogenic properties of MSCs. Therefore, the findings received in this attempt create a fertile base for the setup of cell therapy in patients with AKI.
引用
收藏
页码:284 / 304
页数:21
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